HSPA1B-SLC1A3 Fusion FISH Probe
The HSPA1B-SLC1A3 Fusion FISH Probe is used to confirm a fusion of the HSPA1B and SLC1A3 genes. The fusion of the HSPA1B and SLC1A3 genes has been associated with Brain Lower Grade Glioma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| HSPA1B-SLC1A3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-RERE | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-REOR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-REGO | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-REGR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-REAQ | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-ORRE | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-OROR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-ORGO | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-ORAQ | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GORE | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GOOR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GOGO | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GOGR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GOAQ | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GRRE | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GROR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GRGO | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GRGR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-GRAQ | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-AQRE | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-AQOR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-AQGO | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-AQGR | 20 (40 μL) | 200 μL |
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| HSPA1B-SLC1A3-20-AQAQ | 20 (40 μL) | 200 μL |
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HSPA1B Gene Summary
This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008]
Gene Name: Heat Shock Protein Family A (Hsp70) Member 1B
Chromosome: CHR6_qbl_hap6: 3089162 -3091686
Locus: 6p21.33
SLC1A3 Gene Summary
This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]
Gene Name: Solute Carrier Family 1 Member 3
Chromosome: CHR5: 36606456 -36688436
Locus: 5p13.2
Gene Diseases
The HSPA1B SLC1A3 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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